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rs587778077

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778077(-;-)
Make rs587778077(-;A)
Make rs587778077(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108304830
GeneATM
is asnp
is mentioned by
dbSNPrs587778077
ebirs587778077
HLIrs587778077
Exacrs587778077
Varsomers587778077
Maprs587778077
PheGenIrs587778077
hapmaprs587778077
1000 genomesrs587778077
hgdprs587778077
ensemblrs587778077
gopubmedrs587778077
geneviewrs587778077
scholarrs587778077
googlers587778077
pharmgkbrs587778077
gwascentralrs587778077
openSNPrs587778077
23andMers587778077
23andMe allrs587778077
SNP Nexus

SNPshotrs587778077
SNPdbers587778077
MSV3drs587778077
GWAS Ctlgrs587778077
Max Magnitude0
ClinVar
Risk rs587778077(A;A)
Alt rs587778077(A;A)
Reference rs587778077(;)
Significance Pathogenic
Disease not specified Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN not specified Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108175557dupA
CLNSRC
CLNACC RCV000120144.1, RCV000167879.1,